4.7 Article

One-Dimensional Thiocyanato-Bridged Fe(II) Spin Crossover Cooperative Polymer With Unusual FeN5S Coordination Sphere

期刊

INORGANIC CHEMISTRY
卷 57, 期 19, 页码 12338-12346

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.inorgchem.8b02061

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资金

  1. CNRS (Centre National de la Recherche Scientifique)
  2. Universite de Brest
  3. Agence Nationale de la Recherche (ANR project) [BISTA-MAT: ANR-12-BS07-0030-01]
  4. Junta de Andalucia [FQM-195]
  5. Project of excellence [P11-FQM-7756]
  6. MINECO of Spain [CTQ2014-56312-P]
  7. University of Granada

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We present here a novel example of spin crossover phenomenon on a Fe(II) one-dimensional chain with unusual N5S coordination sphere. The [{Fe(tpc-OMe)(NCS)(mu-NCS)}(n)] (1) compound was prepared using the tridentate tpc-OMe ligand (tpc-OMe = tris(2-pyridyl)methoxymethane), FeCl2 center dot 4H(2)O, and the KSCN salt. Crystallographic investigations revealed that the Fe(II) ions are connected by a single bridging NCS- ligand (mu-kappa N:kappa S-SCN coordination mode) to afford a zigzag neutral chain running along the [010] direction, in which the thiocyanato bridging groups adopt a cis head-to-tail configuration. The (N5S) metal environment arises from one thiocyanato-kappa S and two thiocyanato-kappa N ligands and from three pyridine of the fac-tpc-OMe tripodal ligand. This compound presents a unique extension of Fe(II) binuclear complexes into linear chains built on similar tripodal ligands and bridging thiocyanate anions. Compound 1 shows a spin crossover (SCO) behavior which has been evidenced by magnetic, calorimetric, and structural investigations, revealing a sharp cooperative spin transition with a transition temperature of ca. 199 K. Temperature scan rate studies revealed a very narrow hysteresis loop (similar to 1 K wide). Photoswitching of this compound was also performed, evidencing a very fast relaxation process at low temperature. Among other factors, the linearity of the N-bound terminal thiocyanato ligand appears as the main structural characteristic at the origin of the presence of the SCO transition in compound 1 and in the two others Fe(II) previous systems involving thiocyanato-bridges and tripodal tris(2-pyridyl)methane ligands.

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